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367 related items for PubMed ID: 10995834
1. Cathepsin D deficiency induces lysosomal storage with ceroid lipofuscin in mouse CNS neurons. Koike M, Nakanishi H, Saftig P, Ezaki J, Isahara K, Ohsawa Y, Schulz-Schaeffer W, Watanabe T, Waguri S, Kametaka S, Shibata M, Yamamoto K, Kominami E, Peters C, von Figura K, Uchiyama Y. J Neurosci; 2000 Sep 15; 20(18):6898-906. PubMed ID: 10995834 [Abstract] [Full Text] [Related]
2. Participation of autophagy in storage of lysosomes in neurons from mouse models of neuronal ceroid-lipofuscinoses (Batten disease). Koike M, Shibata M, Waguri S, Yoshimura K, Tanida I, Kominami E, Gotow T, Peters C, von Figura K, Mizushima N, Saftig P, Uchiyama Y. Am J Pathol; 2005 Dec 15; 167(6):1713-28. PubMed ID: 16314482 [Abstract] [Full Text] [Related]
3. Enzyme replacement therapy with recombinant pro-CTSD (cathepsin D) corrects defective proteolysis and autophagy in neuronal ceroid lipofuscinosis. Marques ARA, Di Spiezio A, Thießen N, Schmidt L, Grötzinger J, Lüllmann-Rauch R, Damme M, Storck SE, Pietrzik CU, Fogh J, Bär J, Mikhaylova M, Glatzel M, Bassal M, Bartsch U, Saftig P. Autophagy; 2020 May 15; 16(5):811-825. PubMed ID: 31282275 [Abstract] [Full Text] [Related]
4. Involvement of nitric oxide released from microglia-macrophages in pathological changes of cathepsin D-deficient mice. Nakanishi H, Zhang J, Koike M, Nishioku T, Okamoto Y, Kominami E, von Figura K, Peters C, Yamamoto K, Saftig P, Uchiyama Y. J Neurosci; 2001 Oct 01; 21(19):7526-33. PubMed ID: 11567042 [Abstract] [Full Text] [Related]
5. Lysosomal Storage of Subunit c of Mitochondrial ATP Synthase in Brain-Specific Atp13a2-Deficient Mice. Sato S, Koike M, Funayama M, Ezaki J, Fukuda T, Ueno T, Uchiyama Y, Hattori N. Am J Pathol; 2016 Dec 01; 186(12):3074-3082. PubMed ID: 27770614 [Abstract] [Full Text] [Related]
8. Cathepsin D deficiency induces persistent neurodegeneration in the absence of Bax-dependent apoptosis. Shacka JJ, Klocke BJ, Young C, Shibata M, Olney JW, Uchiyama Y, Saftig P, Roth KA. J Neurosci; 2007 Feb 21; 27(8):2081-90. PubMed ID: 17314303 [Abstract] [Full Text] [Related]
10. Purkinje Cells Are More Vulnerable to the Specific Depletion of Cathepsin D Than to That of Atg7. Koike M, Shibata M, Sunabori T, Yamaguchi J, Sakimura K, Komatsu M, Tanaka K, Uchiyama Y. Am J Pathol; 2017 Jul 21; 187(7):1586-1600. PubMed ID: 28502476 [Abstract] [Full Text] [Related]
11. Cathepsin D in Podocytes Is Important in the Pathogenesis of Proteinuria and CKD. Yamamoto-Nonaka K, Koike M, Asanuma K, Takagi M, Oliva Trejo JA, Seki T, Hidaka T, Ichimura K, Sakai T, Tada N, Ueno T, Uchiyama Y, Tomino Y. J Am Soc Nephrol; 2016 Sep 21; 27(9):2685-700. PubMed ID: 26823550 [Abstract] [Full Text] [Related]
12. Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration. Kasper D, Planells-Cases R, Fuhrmann JC, Scheel O, Zeitz O, Ruether K, Schmitt A, Poët M, Steinfeld R, Schweizer M, Kornak U, Jentsch TJ. EMBO J; 2005 Mar 09; 24(5):1079-91. PubMed ID: 15706348 [Abstract] [Full Text] [Related]
13. Lysosomal storage of the DCCD reactive proteolipid subunit of mitochondrial ATP synthase in human and ovine ceroid lipofuscinoses. Palmer DN, Fearnley IM, Medd SM, Walker JE, Martinus RD, Bayliss SL, Hall NA, Lake BD, Wolfe LS, Jolly RD. Adv Exp Med Biol; 1989 Mar 09; 266():211-22; discussion 223. PubMed ID: 2535017 [Abstract] [Full Text] [Related]
14. Follow-up study of subunit c of mitochondrial ATP synthase (SCMAS) in Batten disease and in unrelated lysosomal disorders. Elleder M, Sokolová J, Hrebícek M. Acta Neuropathol; 1997 Apr 09; 93(4):379-90. PubMed ID: 9113203 [Abstract] [Full Text] [Related]
15. CNS-expressed cathepsin D prevents lymphopenia in a murine model of congenital neuronal ceroid lipofuscinosis. Shevtsova Z, Garrido M, Weishaupt J, Saftig P, Bähr M, Lühder F, Kügler S. Am J Pathol; 2010 Jul 09; 177(1):271-9. PubMed ID: 20489146 [Abstract] [Full Text] [Related]
16. Tripeptidyl peptidase I, the late infantile neuronal ceroid lipofuscinosis gene product, initiates the lysosomal degradation of subunit c of ATP synthase. Ezaki J, Takeda-Ezaki M, Kominami E. J Biochem; 2000 Sep 09; 128(3):509-16. PubMed ID: 10965052 [Abstract] [Full Text] [Related]
17. Developmental changes in the expression of neuronal ceroid lipofuscinoses-linked proteins. Suopanki J, Partanen S, Ezaki J, Baumann M, Kominami E, Tyynelä J. Mol Genet Metab; 2000 Sep 09; 71(1-2):190-4. PubMed ID: 11001810 [Abstract] [Full Text] [Related]
18. Congenital ovine neuronal ceroid lipofuscinosis--a cathepsin D deficiency with increased levels of the inactive enzyme. Tyynelä J, Sohar I, Sleat DE, Gin RM, Donnelly RJ, Baumann M, Haltia M, Lobel P. Eur J Paediatr Neurol; 2001 Sep 09; 5 Suppl A():43-5. PubMed ID: 11589006 [Abstract] [Full Text] [Related]
19. Neuroectoderm-specific deletion of cathepsin D in mice models human inherited neuronal ceroid lipofuscinosis type 10. Ketscher A, Ketterer S, Dollwet-Mack S, Reif U, Reinheckel T. Biochimie; 2016 Mar 09; 122():219-26. PubMed ID: 26232697 [Abstract] [Full Text] [Related]
20. Membrane trafficking and mitochondrial abnormalities precede subunit c deposition in a cerebellar cell model of juvenile neuronal ceroid lipofuscinosis. Fossale E, Wolf P, Espinola JA, Lubicz-Nawrocka T, Teed AM, Gao H, Rigamonti D, Cattaneo E, MacDonald ME, Cotman SL. BMC Neurosci; 2004 Dec 10; 5():57. PubMed ID: 15588329 [Abstract] [Full Text] [Related] Page: [Next] [New Search]